Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance.
Commun Biol
; 7(1): 676, 2024 Jun 03.
Article
in En
| MEDLINE
| ID: mdl-38830954
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Disease Models, Animal
/
Leber Congenital Amaurosis
/
Chaperonin Containing TCP-1
Limits:
Animals
Language:
En
Journal:
Commun Biol
Year:
2024
Document type:
Article
Affiliation country:
Japón
Country of publication:
Reino Unido